Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.28 (T)
Location

Chromosome 7:96655726 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

7:g.96655726T>C

Variation displays